139 positions on this site are linked to Parkinson's Disease, out of 113,826 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
UBAP2 · rs6476434
See detailed info → SensitiveBICD1 · rs77669894
See detailed info → SensitiveHASPIN · rs117672332
See detailed info → SensitiveRP11-162I7 · rs3889108
See detailed info → SensitiveCD19 · rs2904880
See detailed info → SensitiveTEKT4 · rs187989831
See detailed info → SensitiveDLG2 · rs12283611
See detailed info → SensitiveGAK · rs873786
See detailed info → SensitiveLRRK2 · rs190807041
See detailed info → SensitiveNOD2 · rs6500328
See detailed info → SensitiveCHD9 · rs10221156
See detailed info → SensitiveGXYLT1 · rs138017112
See detailed info → SensitiveCRLS1 · rs77351827
See detailed info → SensitiveRPS12 · rs75859381
See detailed info → SensitiveGS1-124K5.11 · rs76949143
See detailed info → SensitiveWDR41 · rs137887044
See detailed info → SensitiveASH1L · rs145330152
See detailed info → SensitiveBST1 · rs12651314
See detailed info → SensitiveKANSL1 · rs113564729
See detailed info → SensitiveGXYLT1 · rs144755950
See detailed info →Showing 20 of 139 · page 4 of 7
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.